State
73,817 recalls have nationwide distribution and so reach US Virgin Islands. 178 additional recalls listed US Virgin Islands specifically in their distribution scope.
Of the 178 recalls naming US Virgin Islands we have scored against our rubric, 12 (7%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 39 (22%) are Severe.
Which agencies issued them
These figures cover only the 178 recalls whose distribution notice names US Virgin Islands specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
The Compounding Pharmacy of America is recalling MIC+Methylcobalamin 4000 mcg/ml Injection due to FDA inspection findings of GMP violations that may impact sterility.
The Compounding Pharmacy of America is recalling Fentanyl and Clonidine Intrathecal Solution due to FDA inspection findings of GMP violations that may impact sterility.
Intuitive Surgical is recalling 1,200 Fluorescence Imaging Procedure Kits because shipping damage may have compromised the sterile packaging of the stopcocks.
St Jude Medical is recalling Merlin@home RF Remote Monitoring Transmitters because some devices exhibit backup VVI operation due to a backup reset.
Boston Scientific is recalling WATCHMAN Access System sheaths because the hemostasis valve may cross-thread if tightened with the dilator in place, potentially preventing the valve from sealing.
Salter Labs is recalling specific NebuTech nebulizer models because the inspiratory valve cap may detach during treatment.
Siemens is recalling ACUSON SC2000 ultrasound systems because a software error prevents the capture of images or clips when patient names are registered with different capitalization.
Boston Scientific is issuing a field correction for WATCHMAN Left Atrial Appendage Closure Devices to prevent hemostasis valve cross-threading and potential blood leakage.
Hospira is recalling 83,320 vials of Ketamine Hydrochloride Injection because customer complaints reported cracked and leaking glass vials.
MedtestDx, Inc. is recalling 79 kits of MedTest DX Control Reconstitution Fluid due to vial fill volume variations that may cause control results to fall outside suggested ranges.
Apotex Inc. is recalling Cevimeline Hydrochloride Capsules, 30 mg, because the product may not meet specification limits for assay testing.
EMD Serono is recalling specific lots of Clomiphene Citrate tablets because the active ingredient failed due to chemical contamination.
RaySearch Laboratories is recalling RayStation software due to a floating-point precision error that affects the display of isodose lines and color tables.
Edwards Lifesciences is recalling pressure monitoring kits due to flow restriction in the IV set, which may prevent system priming or line flushing.
Akorn, Inc. is recalling 370 kits of IC-Green (indocyanine green for injection) because a low out-of-specification potency result was found.
Pointe Scientific is recalling 93 kits of Creatinine Reagent C7539-150 because the R1 and R2 reagent bottles are mislabeled, which prevents valid test results.
Daimler Trucks North America is recalling 2014-2016 Freightliner trucks because rear brake calipers may contact the spring suspension, reducing braking performance.
KYMCO is recalling 2015 Super 8-50 X and Super 8-150 X scooters because the front brake hose may contact the tire, risking brake failure and crashes.
Crossroads is recalling 2015-2016 Sunset Trail trailers because kitchen ranges lack an isolation panel, creating a risk of fire, explosion, or carbon monoxide buildup.
Suzuki is recalling 2012-2013 SX4 vehicles because the power steering pump may seize, causing loss of steering assist and increasing crash risk.
Newmar is recalling specific Dutch Star, Dutch Aire, and King Aire motorhomes because a flexible exhaust tube may tear, allowing hot exhaust to contact other components and increase fire risk.
Michelin is recalling specific X Works XZY tires because they lack required DOT symbols and load range letters, which may cause confusion with non-compliant tires.
Eaton is recalling specific FR-Series 10-speed manual transmissions because the reverse gear may stay engaged, causing the vehicle to move backwards unexpectedly.
Henderson Wheel is recalling torsion arm assemblies where the arm is too small for its housing, posing a risk of trailer detachment and loss of control.
Motor Coach Industries is recalling 145 model year 2015 D4000, D4005, D4500, and D4505 vehicles because an incorrectly assembled fuse block may cause arcing and increase the risk of a fire.